BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 19929407)

  • 21. Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele.
    Gualandi E; Ravani A; Berto A; Burdo S; Trevisi P; Ferlini A; Martini A; Calzolari E
    Acta Otolaryngol Suppl; 2004 May; (552):29-34. PubMed ID: 15219044
    [TBL] [Abstract][Full Text] [Related]  

  • 22. GJB2-associated hearing loss undetected by hearing screening of newborns.
    Minami SB; Mutai H; Nakano A; Arimoto Y; Taiji H; Morimoto N; Sakata H; Adachi N; Masuda S; Sakamoto H; Yoshida H; Tanaka F; Morita N; Sugiuchi T; Kaga K; Matsunaga T
    Gene; 2013 Dec; 532(1):41-5. PubMed ID: 24013081
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spectrum of Genes for Non-
    Shatokhina O; Galeeva N; Stepanova A; Markova T; Lalayants M; Alekseeva N; Tavarkiladze G; Markova T; Bessonova L; Petukhova M; Guseva D; Anisimova I; Polyakov A; Ryzhkova O; Bliznetz E
    Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555390
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations.
    Cascella R; Strafella C; Gambardella S; Longo G; Borgiani P; Sangiuolo F; Novelli G; Giardina E
    Electrophoresis; 2016 Mar; 37(5-6):860-4. PubMed ID: 26681637
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions.
    Bliznetz EA; Lalayants MR; Markova TG; Balanovsky OP; Balanovska EV; Skhalyakho RA; Pocheshkhova EA; Nikitina NV; Voronin SV; Kudryashova EK; Glotov OS; Polyakov AV
    J Hum Genet; 2017 Aug; 62(8):789-795. PubMed ID: 28405014
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
    Tlili A; Al Mutery A; Kamal Eddine Ahmad Mohamed W; Mahfood M; Hadj Kacem H
    Genet Test Mol Biomarkers; 2017 Nov; 21(11):686-691. PubMed ID: 29016196
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The controversial p.Arg127His mutation in GJB2: report on three Portuguese hearing loss family cases.
    Matos TD; Simões-Teixeira H; Caria H; Rosa H; O'Neill A; Fialho G
    Genet Test Mol Biomarkers; 2010 Feb; 14(1):141-4. PubMed ID: 19929408
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar.
    Alkhidir S; El-Akouri K; Al-Dewik N; Khodjet-El-Khil H; Okashah S; Islam N; Ben-Omran T; Al-Shafai M
    Sci Rep; 2024 Feb; 14(1):4202. PubMed ID: 38378725
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
    Norris VW; Arnos KS; Hanks WD; Xia X; Nance WE; Pandya A
    Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns].
    Bliznets EA; Marcul' DN; Khorov OG; Markova TG; Poliakov AV
    Genetika; 2014 Feb; 50(2):214-21. PubMed ID: 25711030
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects.
    Fitzgerald T; Duva S; Ostrer H; Pass K; Oddoux C; Ruben R; Caggana M
    Clin Genet; 2004 Apr; 65(4):338-42. PubMed ID: 15025729
    [TBL] [Abstract][Full Text] [Related]  

  • 32. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
    Abidi O; Boulouiz R; Nahili H; Ridal M; Alami MN; Tlili A; Rouba H; Masmoudi S; Chafik A; Hassar M; Barakat A
    Int J Pediatr Otorhinolaryngol; 2007 Aug; 71(8):1239-45. PubMed ID: 17553572
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two novel missense mutations in the connexin 26 gene in Turkish patients with nonsyndromic hearing loss.
    Yilmaz A; Menevse S; Bayazit Y; Karamert R; Ergin V; Menevse A
    Biochem Genet; 2010 Apr; 48(3-4):248-56. PubMed ID: 19941053
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India.
    Adhikary B; Ghosh S; Paul S; Bankura B; Pattanayak AK; Biswas S; Maity B; Das M
    Gene; 2015 Dec; 573(2):239-45. PubMed ID: 26188157
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
    Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
    JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Connexin26 mutations associated with nonsyndromic hearing loss.
    Park HJ; Hahn SH; Chun YM; Park K; Kim HN
    Laryngoscope; 2000 Sep; 110(9):1535-8. PubMed ID: 10983956
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
    Cryns K; Orzan E; Murgia A; Huygen PL; Moreno F; del Castillo I; Chamberlin GP; Azaiez H; Prasad S; Cucci RA; Leonardi E; Snoeckx RL; Govaerts PJ; Van de Heyning PH; Van de Heyning CM; Smith RJ; Van Camp G
    J Med Genet; 2004 Mar; 41(3):147-54. PubMed ID: 14985372
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Analysis and prenatal diagnosis of deafness-related gene mutations in patients with nonsyndromic hearing loss].
    Li H; Chen Y; Mao Y; Ding Y; Xu X; Tang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):553-6. PubMed ID: 25297579
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.
    del Castillo I; Villamar M; Moreno-Pelayo MA; del Castillo FJ; Alvarez A; Tellería D; Menéndez I; Moreno F
    N Engl J Med; 2002 Jan; 346(4):243-9. PubMed ID: 11807148
    [TBL] [Abstract][Full Text] [Related]  

  • 40. GJB2 mutations are rare in probands with hearing loss in Chinese assortative mating families.
    Chen G; Liu J; Dong J; Li J; Fu S
    Int J Pediatr Otorhinolaryngol; 2014 Feb; 78(2):244-7. PubMed ID: 24359977
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.